| Polyarticular pigmented villonodular synovitis associated with multiple congenital anomalies. A case of Noonan-like/multiple giant cell lesion syndrome. | |
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MedLine Citation:
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PMID: 8737730 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A case of polyarticular pigmented villonodular synovitis associated with many congenital phenotypic peculiarities (such as shortness, blue sclerae, flattened nose, low-set ears, hypertelorism, curly hair and pulmonary stenosis) is described. The presence of many of the typical signs of the Noonan syndrome and the histological finding of giant cells on the synovial biopsy led to the diagnosis of Noonan-like/multiple giant cell lesion syndrome. |
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Authors:
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G Minisola; V Porzio; F Ceralli; L R Grillo; F Porzio |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Clinical and experimental rheumatology Volume: 14 ISSN: 0392-856X ISO Abbreviation: Clin. Exp. Rheumatol. Publication Date: 1996 Mar-Apr |
Date Detail:
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Created Date: 1996-12-09 Completed Date: 1996-12-09 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 8308521 Medline TA: Clin Exp Rheumatol Country: ITALY |
Other Details:
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Languages: eng Pagination: 207-10 Citation Subset: IM |
Affiliation:
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Department of Rheumatology, Sandro Pertini Hospital, Azienda USL Roma B, Rome, Italy. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple
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pathology* Adolescent Female Giant Cells / pathology* Humans Noonan Syndrome / pathology* Syndrome Synovitis, Pigmented Villonodular / complications*, pathology*, radiography |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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